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Idiopathic pulmonary fibrosis: current treatment options and critical appraisal of nintedanib

Idiopathic pulmonary fibrosis (IPF) is the most common type of idiopathic interstitial pneumonia and is characterized by a poor prognosis, with an estimated 5-year survival of approximately 20%. Progressive and irreversible lung functional impairment leads to chronic respiratory insufficiency with a...

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Dettagli Bibliografici
Pubblicato in:Drug Des Devel Ther
Autori principali: Bonella, Francesco, Stowasser, Susanne, Wollin, Lutz
Natura: Artigo
Lingua:Inglês
Pubblicazione: Dove Medical Press 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4686227/
https://ncbi.nlm.nih.gov/pubmed/26715838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DDDT.S76648
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